analyzing changes in lignin chemistry due to biofuel ... · how to determine frs lignin chemistry?...
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Analyzing Changes in Lignin Chemistry Due to BiofuelProduction Processes
S. Carter FoxWeyerhaeuser
I Seattle, WA I April 30, 2014Northwest Wood-Based Biofuels
+ Co-Products Conference
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NARA Supply Chain
Image credit: NARA2
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Source of Lignin in a Biorefinery
Image from: Alonso, D. M.; Wettstein, S. G.; Dumesic, J. A. Chem. Soc. Rev. 2012, 41, 8075-8098.
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The Need for Co-ProductsR
elat
ive
IPK
Pro
duct
ion
Cos
t
2.88 0.73
Credit: Gevan Marrs, NARA
0.04 0.170.06 0.15
1.75
Speculative – need to be developed
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Few Commercial Uses for Lignin
• Annual lignin production:– 40 to 50 million metric tons?
• Annual commercial lignin consumption:– ≈ 1.5 million metric tons
• What is the problem? Why isn’t lignin more widely used?
• Are the chances for success in lignin utilization better today?
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Lignin Complexity
• Lignin is a complex molecule to begin with.
Ref: Zakzeski, J., et al., Chem. Rev. 2010, 110, 3552-3599.
OOCH3
OHO
OH
HO
O
OCH3O
OH
OCH3
O
O
HO
OCH3
HO
O
OH
OH
OHO
OCH3
O
O
OH
OCH3
OCH3
HO
HO
O
HO
OOH
OCH3
HO
HO
H3CO
O
OCH3
HOO
HO
H3CO
OHO
HO
OCH3
O
O
O
OH
OH
HOH3CO
OHOCH3
HOO
HO
O
OH
OH
H3CO
O OH
O
HO OCH3
O
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Lignin Isolation Affects its Structure and Purity
• Commercial– Kraft pulping– Sulfite pulping
• Non-commercial– Organosolve pulping– Milled wood– Ionic liquid pretreatment– Mild acid hydrolysis
Photo credit: JBEI7
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Drivers for Success
Near Term• Cleaner commercial lignins• Characterization methods are more
powerful• New market opportunities
Long Term• Better methods to break specific
lignin bonds• Advances in biomass fractionation• Ability to manipulate lignin
biosynthesis8
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Many Possibilities from Lignin
Fine Chemicals
Fuels
Carbon Products
Thermoplastics
Energy Storage
Adsorbents
Rubber Reinforcement
Phenolic Resins
Concrete Dispersant
Lignin
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NARA Supply Chain
Image credit: NARA10
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NARA Co-Product Streams
Wood Chips or Forest Residuals
Spent Sulfite Liquor
Residual SolidsResidual Solids
MBS Process
Treated Wood
Enzyme Hydrolysis & Fermentation
WOx Process
Treated Wood
Enzyme Hydrolysis & Fermentation
Soluble Sugars to Fermentation
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Mild Bisulfite Pretreatment (MBS)
Process development by Johnway Gao and Dwight Anderson at Catchlight Energy and J.Y. Zhu at the Forest Products Laboratory
Refs: Zhang, C., et al. BioEnergy Research. 2012, 5, 978-988.Gao, J., et al. Biotechnology for Biofuels 2013, 6, 10.
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Wet Oxidation Pretreatment
Elevated temperature& pressure
O2 + steam
Flash Tank
LigninHemicellulose
Cellulose
Contains all wood components
Process development by Dr. Brigitte Ahring at Washington State University’s Bioproducts, Sciences & Engineering Laboratory
Ref: Rana, D., et al. Bioresour. Technol. 2012, 121, 61-67.
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Composition of Fermentation Residual Solids (FRS)
Sample Total Klason Lignin Total Polysaccharide Ash Sulfur
Feedstock 34.9% 54.4% 0.2% 0.0%
MBS FRSas rec’d 70.4% 18.9% 8.9% 2.4%
MBS FRS washed 69.4% 23.9% 4.1% 1.8%
Wet Ox FRSas rec’d 53.0% 43.9% 2.0% 0.1%
Wet Ox FRS washed 53.4% 47.3% 0.5% 0.0%
% oven dry
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How to Determine FRS Lignin Chemistry?
‒ Saccharification and fermentation residual solids are insoluble in all attempted solvents.
‒ Need to extract high purity, unmodified lignin from SRS and FRS samples.
‒ Can we simply extract lignin using dioxane/water mixture, similar to milled wood lignin?
‒ Not really.
Sample Yield
MBS SRS 2.8%
Wet Ox SRS 8.3%
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Ball Milling Increases Extracted Lignin Yield
0%
5%
10%
15%
20%
25%
0 100 200 300
Isol
ated
Yie
ld
Ball Milling Time (h)
Effect of Ball Milling on Lignin Isolationfrom Wet Ox SRS
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Enzymatic Mild Acidolysis Lignin (EMAL)
Procedure developed by the Argyropoulos research group at NC State. (Ref: Guerra, A., et al. J. Agric. Food. Chem. 2006, 54, 5939-5947.)
Ball Milling21 days
Enzymatic Hydrolysis48 hours
Solvent Extraction2 hours
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Lignin Isolation Yields
Sample Enzymatic Hydrolysis Yield
Lignin ExtractionYield
Extracted LigninPurity
Forest Residuals 42.8% 52.4% 81.0%
Mild Bisulfite FRS 64.7% 52.5% 95.4%
Wet Oxidation FRS 86.4% 44.9% 94.2%
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Lignosulfonate Isolation Procedure
Spent SulfiteLiquor
C12H25NH3in octanol aqueous NaOH
Organic extraction
Discard
Organic PhaseLS/amine complex
AqueousPhaseResidualsugars,
salts
Retain and dry
Back extraction
Organic PhaseDodecylamine
AqueousPhaseNa+ LS
Ref: Ringena, O., et al. Holzforschung 2005, 59, 405-412.19
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Elemental Analysis of Isolated Lignins
Sample Sulfur Carbon Hydrogen Nitrogen Oxygen*
Forest Residual Lignin 0.032 61.0 6.0 0.07 32.9
Wet Oxidation Lignin 0.096 64.9 5.3 0.96 28.7
Mild Bisulfite Lignin 1.13 63.3 5.7 1.01 28.9
MBS Lignosulfonic acid 8.10 52.1 4.8 0.36 34.7
* Oxygen determined by differenceAll values % oven dry
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31P NMR Analysis of EMALs
125130135140145150155ppm
aliphatic OHinternal standard
phenolic OH
COOH
guaiacylTMDP
hydrolysis product
C-5 substituted
Cl PO
OCH3
CH3
CH3
CH3
Lignin OH + Lignin O PO
OCH3
CH3
CH3
CH3
+ ClH
Quant. 31P NMR spectrum of forest harvest residual EMAL21
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Hydroxyl Group Comparison
Sample Aliphatic OH Aromatic OH C-5 Substituted OH COOH
Forest ResidualsLignin 4.31 1.11 1.45 0.03
Wet Oxidation Lignin 1.93 2.86 1.32 0.21
Mild Bisulfite Lignin 1.38 2.71 1.66 0.22
MBS Lignosulfonic acid 2.42 3.96 1.73 0.10
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Molecular Weight Analysis
Sample Mn Mw PDI
Forest Residuals Lignin 26.8 ± 54.6 1.94
Wet Oxidation Lignin 34.1 ± 45.7 1.34
Mild Bisulfite Lignin 47.5 56.4 1.19
MBS Lignosulfonic acid 4.7 28.0 5.92
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Summary
• Developing value-added products from lignin-rich process residuals will be critical to large scale biorefinery commercial success.
• Different pretreatment technologies produce residuals with different properties.
• The residues from Mild Bisulfite and Wet Oxidation pretreatments contain a lot more than just lignin.
• Processes to upgrade lignin must be robust enough to handle significant impurity content and variability in the feedstock.
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Summary
• High purity lignin was isolated from the Mild Bisulfite and Wet Oxidation residuals and characterized with respect to elemental content, hydroxyl group content, and molecular weight
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Acknowledgements
• Colleagues Dave Fish and Ian Dallmeyer• NARA Summer undergraduate intern Steve Cline
• NARA is primarily supported by an Agriculture and Food Research Initiative Competitive Grant no. 2011-68005-30416 from the USDA National Institute of Food and Agriculture.
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